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Items: 1 to 20 of 2820

1.

Graph coloring for extracting discriminative genes in cancer data.

Mahfouz MA, Nepomuceno JA.

Ann Hum Genet. 2019 Jan 15. doi: 10.1111/ahg.12297. [Epub ahead of print]

PMID:
30644085
2.

Genetic variations and population data on five supplementary STR markers in Lebanon.

Andari AE, Mourad L, Mansour I.

Ann Hum Genet. 2018 Nov 22. doi: 10.1111/ahg.12292. [Epub ahead of print]

PMID:
30565662
3.
4.

Population genetics of 19 Y-STR loci in Yanbian Korean samples from China.

Xuan JF, Adnan A, Khan RA, Xing JX, Yao J, Wang BJ.

Ann Hum Genet. 2018 Dec 2. doi: 10.1111/ahg.12296. [Epub ahead of print]

PMID:
30506867
5.

Expression patterns common and unique to ulcerative colitis and celiac disease.

Medrano LM, Pascual V, Bodas A, López-Palacios N, Salazar I, Espino-Paisán L, González-Pérez B, Urcelay E, Mendoza JL, Núñez C.

Ann Hum Genet. 2018 Nov 6. doi: 10.1111/ahg.12293. [Epub ahead of print]

PMID:
30402962
6.

Diagnostic approach with genetic tests for global developmental delay and/or intellectual disability: Single tertiary center experience.

Han JY, Jang W, Park J, Kim M, Kim Y, Lee IG.

Ann Hum Genet. 2018 Nov 6. doi: 10.1111/ahg.12294. [Epub ahead of print]

PMID:
30402882
7.

IL8 and IL17A polymorphisms associated with multibacillary leprosy and reaction type 1 in a mixed population from southern Brazil.

Aquino JS, Ambrosio-Albuquerque EP, Alves HV, Macedo LC, Visentainer L, Sell AM, Visentainer JEL.

Ann Hum Genet. 2018 Oct 10. doi: 10.1111/ahg.12291. [Epub ahead of print]

PMID:
30303246
8.

Confirmation of BRD4 haploinsufficiency role in Cornelia de Lange-like phenotype and delineation of a 19p13.12p13.11 gene contiguous syndrome.

Alesi V, Dentici ML, Loddo S, Genovese S, Orlando V, Calacci C, Pompili D, Dallapiccola B, Digilio MC, Novelli A.

Ann Hum Genet. 2018 Oct 10. doi: 10.1111/ahg.12289. [Epub ahead of print]

PMID:
30302754
9.

A novel heterozygous variant p.(Trp538Arg) of SYNM is identified by whole-exome sequencing in a Chinese family with dilated cardiomyopathy.

Zhang SB, Liu YX, Fan LL, Huang H, Li JJ, Jin JY, Xiang R.

Ann Hum Genet. 2018 Oct 2. doi: 10.1111/ahg.12287. [Epub ahead of print]

PMID:
30276801
10.

Adaptation to milking agropastoralism in Chilean goat herders and nutritional benefit of lactase persistence.

Montalva N, Adhikari K, Liebert A, Mendoza-Revilla J, Flores SV, Mace R, Swallow DM.

Ann Hum Genet. 2019 Jan;83(1):11-22. doi: 10.1111/ahg.12277. Epub 2018 Sep 27.

PMID:
30264486
11.

A PEAR1 polymorphism (rs12041331) is associated with risk of coronary artery aneurysm in Kawasaki disease.

Pi L, Xu Y, Fu L, Zhang L, Liu Y, Zhou H, Che D, Gu X.

Ann Hum Genet. 2019 Jan;83(1):54-62. doi: 10.1111/ahg.12285. Epub 2018 Sep 7.

PMID:
30256383
12.

DYNC1H1 gene methylation correlates with severity of spinal muscular atrophy.

Maretina M, Egorova A, Baranov V, Kiselev A.

Ann Hum Genet. 2018 Sep 24. doi: 10.1111/ahg.12288. [Epub ahead of print]

PMID:
30246859
13.

The rs2516839 variation of USF1 gene is associated with 4-year mortality of nonagenarian women: The Vitality 90+ study.

Ozsait-Selcuk B, Komurcu-Bayrak E, Jylhä M, Luukkaala T, Perola M, Kristiansson K, Mononen N, Hurme M, Kähönen M, Goebeler S, Laaksonen R, Hervonen A, Erginel-Unaltuna N, Karhunen PJ, Lehtimäki T.

Ann Hum Genet. 2019 Jan;83(1):34-45. doi: 10.1111/ahg.12282. Epub 2018 Sep 11.

PMID:
30203836
14.

Genetic polymorphisms, forensic efficiency, and phylogenetic analysis of 15 autosomal STR loci in the Uygur population of Ili Kazakh Autonomous Prefecture, Northwestern China.

Feng CM, Wang X, Yu H, Wang XL, Zhang GH.

Ann Hum Genet. 2019 Jan;83(1):46-53. doi: 10.1111/ahg.12283. Epub 2018 Sep 7.

PMID:
30191965
15.

Association of polymorphisms in genes coding for antioxidant enzymes and human male infertility.

García Rodríguez A, de la Casa M, Johnston S, Gosálvez J, Roy R.

Ann Hum Genet. 2019 Jan;83(1):63-72. doi: 10.1111/ahg.12286. Epub 2018 Sep 7.

PMID:
30191955
16.

Assessment of candidate folate sensitive-differentially methylated regions in a randomised controlled trial of continued folic acid supplementation during the second and third trimesters of pregnancy.

Harrison A, Pentieva K, Ozaki M, McNulty H, Parle-McDermott A.

Ann Hum Genet. 2019 Jan;83(1):23-33. doi: 10.1111/ahg.12281. Epub 2018 Sep 3.

PMID:
30175844
17.

Update of spectrum c.35delG and c.-23+1G>A mutations on the GJB2 gene in individuals with autosomal recessive nonsyndromic hearing loss.

Azadegan-Dehkordi F, Ahmadi R, Koohiyan M, Hashemzadeh-Chaleshtori M.

Ann Hum Genet. 2019 Jan;83(1):1-10. doi: 10.1111/ahg.12284. Epub 2018 Sep 3. Review.

PMID:
30175840
18.

Deletion at 12q12 increases the risk of developmental delay and intellectual disability.

Weng Y, Luo X, Hou L.

Ann Hum Genet. 2018 Nov;82(6):482-487. doi: 10.1111/ahg.12279. Epub 2018 Aug 29.

19.

Genotype-phenotype correlation and the size of microdeletion or microduplication of 7q11.23 region in patients with Williams-Beuren syndrome.

Ghaffari M, Tahmasebi Birgani M, Kariminejad R, Saberi A.

Ann Hum Genet. 2018 Nov;82(6):469-476. doi: 10.1111/ahg.12278. Epub 2018 Aug 29.

PMID:
30155880
20.

Genetic role of CYP4A11 polymorphisms in the risk of developing cardiovascular and cerebrovascular diseases.

Yu K, Zhang T, Li X.

Ann Hum Genet. 2018 Nov;82(6):370-381. doi: 10.1111/ahg.12280. Epub 2018 Aug 22.

PMID:
30132788

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